Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0013362
Disease: Dysarthria
Dysarthria 		487 0 36 7.0E-02 0 0
CUI: C0028968
Disease: Olivopontocerebellar Atrophies
Olivopontocerebellar Atrophies 		28 0 6 7.0E-02 0 0
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		122 0 12 6.9E-02 0 0
CUI: C0035613
Disease: Rift Valley Fever
Rift Valley Fever 		45 0 7 6.9E-02 0 0
CUI: C0206631
Disease: Lipomatous neoplasm
Lipomatous neoplasm 		14 0 5 6.8E-02 0 0
CUI: C0333440
Disease: Hyaline body
Hyaline body 		14 0 5 6.8E-02 0 0
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign 		155 0 14 6.8E-02 0 0
CUI: C0272401
Disease: Virchow's node (disorder)
Virchow's node (disorder) 		30 0 6 6.8E-02 0 0
CUI: C4721773
Disease: Postoperative cognitive dysfunction
Postoperative cognitive dysfunction 		93 0 10 6.8E-02 0 0
CUI: C0234366
Disease: Ataxic
Ataxic 		15 0 5 6.8E-02 0 0
CUI: C0221292
Disease: Basophilic leukemia
Basophilic leukemia 		32 0 6 6.7E-02 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 14 6.5E-02 0 0
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE 		18 0 5 6.5E-02 0 0
CUI: C4042861
Disease: Obesity, Metabolically Benign
Obesity, Metabolically Benign 		19 0 5 6.4E-02 0 0
CUI: C0085166
Disease: Bacterial Vaginosis
Bacterial Vaginosis 		73 0 8 6.2E-02 0 0
CUI: C1408507
Disease: Supranuclear ophthalmoplegia
Supranuclear ophthalmoplegia 		5 0 4 6.2E-02 0 0
CUI: C0751783
Disease: Lafora Disease
Lafora Disease 		92 0 9 6.1E-02 0 0
CUI: C0012569
Disease: Diplopia
Diplopia 		75 0 8 6.1E-02 0 0
CUI: C0270749
Disease: Marie Cerebellar Ataxia
Marie Cerebellar Ataxia 		6 0 4 6.1E-02 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination 		59 0 7 6.0E-02 0 0
CUI: C0018790
Disease: Cardiac Arrest
Cardiac Arrest 		411 0 27 6.0E-02 0 0
CUI: C1843921
Disease: Postural instability
Postural instability 		60 0 7 6.0E-02 0 0
CUI: C0263661
Disease: Disorder of skeletal system
Disorder of skeletal system 		25 0 5 6.0E-02 0 0
CUI: C1837458
Disease: Impaired smooth pursuit
Impaired smooth pursuit 		25 0 5 6.0E-02 0 0
CUI: C1859807
Disease: AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder) 		25 0 5 6.0E-02 0 0